BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

    QWIK-1(TM) IN-LINE IV FLUID WARMER

    K Number: K914867 · Decision Oct 23, 1992
    View on FDA
    Classifications
    1
    FEI Numbers
    71
    Registration Numbers
    71
    Same Product Code
    74
    Applicant Total
    5
    Review Days
    360

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    Basic Information

    Device Name
    QWIK-1(TM) IN-LINE IV FLUID WARMER
    K Number
    K914867
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    880.5725
    Medical Specialty
    General Hospital
    Decision
    Substantially Equivalent
    Statement or Summary
    Statement
    Applicant
    Microwave Medical Systems, Inc.
    Date Received
    October 29, 1991
    Decision Date
    October 23, 1992
    Product Code
    LGZ
    Advisory Committee
    General Hospital
    Review Advisory Committee
    HO
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    LGZ Warmer, Thermal, Infusion Fluid

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